Canonical Allele Identifier: CA375776912

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140671263C>A (hg19) ; chr9:g.137776811C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137776811C>A , CM000671.2:g.137776811C>A	GRCh38
NC_000009.11:g.140671263C>A , CM000671.1:g.140671263C>A	GRCh37
NC_000009.10:g.139791084C>A	NCBI36
NG_011776.1:g.162820C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.1985C>A MANE Select	ENSP00000417980.1:p.Ala662Asp
ENST00000636027.1:c.1871C>A	ENSP00000489961.1:p.Ala624Asp
ENST00000637161.1:c.1892C>A	ENSP00000490328.1:p.Ala631Asp
ENST00000637261.1:c.2025C>A	ENSP00000490815.1:n.2025C>A
ENST00000638071.1:c.1612C>A
ENST00000640639.1:c.1154C>A	ENSP00000491823.1:p.Ala385Asp
ENST00000371394.6:c.*1720C>A	ENSP00000485945.1:n.*1720C>A
ENST00000460843.5:c.1985C>A	ENSP00000417980.1:p.Ala662Asp
ENST00000462484.5:c.1985C>A	ENSP00000417328.1:p.Ala662Asp
ENST00000462942.3:c.842C>A	ENSP00000436107.1:p.Ala281Asp
ENST00000626603.1:n.1638G>T
NM_001145527.1:c.1985C>A	NP_001138999.1:p.Ala662Asp
NM_024757.4:c.1985C>A	NP_079033.4:p.Ala662Asp
XM_005266105.3:c.1976C>A	XP_005266162.1:p.Ala659Asp
XM_005266110.1:c.1892C>A	XP_005266167.1:p.Ala631Asp
XM_006717288.2:c.1967C>A	XP_006717351.1:p.Ala656Asp
XM_011519021.1:c.1994C>A	XP_011517323.1:p.Ala665Asp
XM_011519022.1:c.1991C>A	XP_011517324.1:p.Ala664Asp
XM_011519023.1:c.1973C>A	XP_011517325.1:p.Ala658Asp
XM_011519024.1:c.1916C>A	XP_011517326.1:p.Ala639Asp
XM_011519025.1:c.1892C>A	XP_011517327.1:p.Ala631Asp
XM_011519026.1:c.1850C>A	XP_011517328.1:p.Ala617Asp
XM_011519027.1:c.1994C>A	XP_011517329.1:p.Ala665Asp
XM_011519028.1:c.1994C>A	XP_011517330.1:p.Ala665Asp
XM_011519029.1:c.416C>A	XP_011517331.1:p.Ala139Asp
XM_011519033.1:c.1829C>A	XP_011517335.1:p.Ala610Asp
NM_001354259.1:c.1892C>A	NP_001341188.1:p.Ala631Asp
NM_001354263.1:c.1964C>A	NP_001341192.1:p.Ala655Asp
XM_005266105.5:c.1976C>A	XP_005266162.1:p.Ala659Asp
XM_011519021.3:c.1994C>A	XP_011517323.1:p.Ala665Asp
XM_011519022.3:c.1991C>A	XP_011517324.1:p.Ala664Asp
XM_011519023.3:c.1973C>A	XP_011517325.1:p.Ala658Asp
XM_011519029.3:c.416C>A	XP_011517331.1:p.Ala139Asp
XM_017015134.1:c.1970C>A	XP_016870623.1:p.Ala657Asp
XM_017015136.2:c.1886C>A	XP_016870625.1:p.Ala629Asp
XM_017015137.1:c.1871C>A	XP_016870626.1:p.Ala624Asp
XM_017015138.1:c.1871C>A	XP_016870627.1:p.Ala624Asp
XM_024447674.1:c.1814C>A	XP_024303442.1:p.Ala605Asp
XM_024447675.1:c.1748C>A	XP_024303443.1:p.Ala583Asp
XM_024447676.1:c.1109C>A	XP_024303444.1:p.Ala370Asp
XM_024447677.1:c.1109C>A	XP_024303445.1:p.Ala370Asp
XM_024447678.1:c.1892C>A	XP_024303446.1:p.Ala631Asp
XM_024447679.1:c.1892C>A	XP_024303447.1:p.Ala631Asp
XM_024447680.1:c.1727C>A	XP_024303448.1:p.Ala576Asp
NM_024757.5:c.1985C>A MANE Select	NP_079033.4:p.Ala662Asp
NM_001145527.2:c.1985C>A	NP_001138999.1:p.Ala662Asp
NM_001354259.2:c.1892C>A	NP_001341188.1:p.Ala631Asp
NM_001354263.2:c.1964C>A	NP_001341192.1:p.Ala655Asp